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Dermatitis, Atopic clinical trials

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NCT ID: NCT00185510 Completed - Dermatitis, Atopic Clinical Trials

Efficacy and Safety Study of Advantan for Maintenance Treatment of Atopic Dermatitis

Start date: March 2005
Phase: Phase 4
Study type: Interventional

Purpose of the study: One bothering feature of atopic dermatitis is its relapsing nature. Hence, it is worthwhile to test modes how to efficiently prevent relapses or at least increase the time until the disease recurs. In order to give recommendations to other patients, this study is to scientifically describe efficacy and safety of a given regimen, namely a maintenance therapy with two days a week Advantan.

NCT ID: NCT00180141 Completed - Atopic Dermatitis Clinical Trials

Elidel-Study: Elidel in Patients With Atopic Dermatitis

Start date: April 2005
Phase: Phase 4
Study type: Interventional

Atopic dermatitis is a common disease. Emollients and Elidel have both shown to be effective to treat this disease. The research question is, whether the effective component (Elidel) is better than the emollient to improve the skin function.

NCT ID: NCT00179959 Completed - Atopic Dermatitis Clinical Trials

The Impact of Treating Staphylococcus Aureus Infection and Colonization on the Clinical Severity of Atopic Dermatitis

Start date: September 2005
Phase: Phase 4
Study type: Interventional

Staphylococcus aureus (S. aureus) infection is perceived not only as a common secondary complication of atopic dermatitis (AD), but also as a culprit in the worsening of this condition. In addition, the recent development of community acquired methicillin-resistant S. aureus (CA-MRSA) has presented a new challenge to our management of AD, both in treatment of acute infections and maintenance therapy. The investigators would like to perform a randomized investigator-blinded placebo-controlled study of children aged 6 months to 17 years with moderate to severe atopic dermatitis with clinical signs of secondary bacterial infection to study: 1) the prevalence of CA-MRSA in our patient population; 2) the relationship of sensitivity of the S. aureus organism cultured from the infected lesion(s) to clinical response to oral cephalexin therapy and severity of the AD; and 3) whether concurrent treatment of S. aureus infection initially with nasal mupirocin ointment and sodium hypochlorite (bleach) baths can result in long-term S. aureus eradication and clinical stability.

NCT ID: NCT00167752 Completed - Psoriasis Clinical Trials

Psychiatric Problems in Chronic Skin Diseases

Start date: December 2002
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the prevalence of depression, anxiety, and sleep problems in patients with chronic skin diseases in dermatology clinics at the University of Wisconsin Hospital and Clinics.

NCT ID: NCT00159523 Completed - Asthma Clinical Trials

Impact in Off-spring of Mothers After Perinatal Daily Intake of a Probiotic

Start date: December 2003
Phase: N/A
Study type: Interventional

A probiotic (Lactobacillus rhamnosus GG) supplement to pregnant women the last four weeks of pregnancy and three months after birth is expected to give a 40% reduction in risk of atopic sensitisation and allergic disease at two years of age, compared to placebo.

NCT ID: NCT00152464 Completed - Dermatitis, Atopic Clinical Trials

Prevention of Asthma With Levocetirizine 18 Month Treatment in Infants (12 - 24 Months) Suffering From Eczema (Atopic Dermatitis) and Sensitized to Grass Pollen and/or House Dust Mite (HDM)

Start date: March 20, 2002
Phase: Phase 3
Study type: Interventional

The Early Prevention of Asthma in Atopic Children (EPAAC™). 24 months study to evaluate the efficacy and safety of levocetirizine (LCTZ) in preventing the onset of asthma in 12 to 24 months old children.

NCT ID: NCT00150059 Completed - Atopic Dermatitis Clinical Trials

Efficacy and Safety of Pimecrolimus Cream 1% in Patients ≥ 3 Months of Age With Mild or Moderate Atopic Dermatitis

Start date: December 2004
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy and safety of pimecrolimus cream 1% in its registered indication (treatment of patients > 3 months of age with mild to moderate atopic dermatitis) This study is not enrolling patients in the United States.

NCT ID: NCT00148746 Completed - Clinical trials for Moderate to Severe Atopic Dermatitis

Standardized Time- and Score-oriented Treatment of Moderate and Severe Atopic Dermatitis

Start date: May 2004
Phase: N/A
Study type: Interventional

The study was designed to test the hypothesis whether a standardized, time-and score-oriented treatment following a strict evidence based algorithm is equally effective to a standard treatment regimen for moderate to severe atopic dermatitis. Study Type: Mono-centre study, patients are blinded, physicians are randomized to either treat study- or controll group Eligible are patients age 2 years or older with SCORAD >= 20 Duration: 12 Months, study visits every 4 weeks. Primary endpoint is Difference between Baseline SCORAD and mean SCORAD under treatment. Secundary endpoints are quality of life, safety and economic burden in both treatment groups.

NCT ID: NCT00146003 Completed - Dermatitis, Atopic Clinical Trials

Efalizumab for Eczema

Start date: March 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to demonstrate a measurable improvement on a validated scale in a small population of adult patients with atopic dermatitis (eczema).

NCT ID: NCT00139581 Completed - Atopic Dermatitis Clinical Trials

Comparison of Pimecrolimus Cream 1% Twice-Daily to Once-Daily Dosing in the Management of Atopic Dermatitis in Pediatric Subjects

Start date: September 2004
Phase: Phase 4
Study type: Interventional

This study is not being conducted in the United States. To investigate the relative efficacy of pimecrolimus cream 1% applied twice daily (b.i.d.) versus once daily (o.d.) in preventing the progression to disease "relapse".